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Empirical substitution models of protein evolution: database, relationships, and modeling considerations.

作者信息

Iglesias-Rivas Paula, Del Amparo Roberto, Cabaleiro Javier A, Arenas Miguel

机构信息

CINBIO, Universidade de Vigo, 36310 Vigo, Spain.

Department of Biochemistry, Genetics and Immunology, Universidade de Vigo, 36310 Vigo, Spain.

出版信息

Database (Oxford). 2025 Jan 18;2025. doi: 10.1093/database/baaf052.

DOI:10.1093/database/baaf052
PMID:40996708
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12462380/
Abstract

Substitution models of protein evolution describe the patterns of amino acid substitutions over evolutionary time and are fundamental for probabilistic methods of phylogenetic inference. At the protein level, a variety of substitution models are available, but only empirical substitution models are well established in phylogenetics due to their mathematical simplicity. Despite their importance, a database compiling the large number of currently available empirical substitution models of protein evolution is lacking, although such a resource could facilitate access, assessment, and subsequent implementation of these models into phylogenetic frameworks. Besides, little is known about formal comparisons between the current set of empirical substitution models. We present EModelDB, a database of empirical substitution models of protein evolution required for probabilistic protein phylogenetics that includes the corresponding exchangeability matrices, model classification, and model-specific biological information. The database is integrated into a graphical user interface, written in Python and SQL, that facilitates its usability. We also compared common empirical substitution models in terms of the distance between their relative rates of amino acid substitution and amino frequencies at equilibrium. We found that substitution models derived from proteins related in nature tend to cluster together, reflecting similar evolutionary patterns. Indeed, we evaluated the empirical substitution models in terms of the folding stability of the derived modeled proteins and found that they generally produce less stable proteins compared to real proteins, suggesting that substitution models with additional evolutionary constraints can be preferred for studying protein evolution accounting for folding stability. Database URL: https://github.com/Paula-Iglesias-Rivas/EModelDB.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7ed/12462380/1c6dd599ecfe/baaf052fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7ed/12462380/928821d195f1/baaf052fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7ed/12462380/e79bb4940b41/baaf052fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7ed/12462380/1c6dd599ecfe/baaf052fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7ed/12462380/928821d195f1/baaf052fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7ed/12462380/e79bb4940b41/baaf052fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7ed/12462380/1c6dd599ecfe/baaf052fig3.jpg

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